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941.
Sedaghati Saeb Azizian Homa Montazer Mohammad Nazari Mohammadi-Khanaposhtani Maryam Asadi Mehdi Moradkhani Fatemeh Ardestani Mehdi Shafiee Asgari Mohammad Sadegh Yahya-Meymandi Azadeh Biglar Mahmood Larijani Bagher Sadat-Ebrahimi Seyed Esmaeil Foroumadi Alireza Amanlou Massoud Mahdavi Mohammad 《Structural chemistry》2021,32(1):37-48
Structural Chemistry - A novel series of (thio)barbituric-phenoxy-N-phenylacetamide derivatives 7a-l was synthesized and evaluated against Helicobacter pylori urease. The latter assay revealed that... 相似文献
942.
Sahar Rohani Ghodsi Mohammadi Ziarani Alireza Badiei Abolfazl Ziarati Maryam Jafari Alireza Shayesteh 《应用有机金属化学》2018,32(8)
Modification of mesoporous silica was carried out by reaction of SBA‐15 with di‐urea‐based ligand. Next, with the help of this ligand, palladium ions were anchored within the multidentate SBA‐15/di‐urea pore channels with high dispersion. The SBA‐15/di‐urea/Pd catalyst was characterized using various techniques. Theoretical calculations indicated that each palladium ion was strongly interacted with one nitrogen and two oxygen atoms from the multidentate di‐urea ligand located in SBA‐15 channels and these interactions remained during the catalytic cycle. These results are in good agreement with those of hot filtration test: the palladium ions have very high stability against leaching from the SBA‐15/di‐urea support. The catalytic performance of SBA‐15/di‐urea/Pd nanostructure was examined for the Suzuki coupling reaction of phenylboronic acid and electronically diverse aryl halides under mild conditions with a minimal amount of Pd (0.26 mol%). Compared to previous reports, this protocol afforded some advantages such as short reaction times, high yields of products, catalyst stability without leaching, easy catalyst recovery and preservation of catalytic activity for at least six successive runs. 相似文献
943.
Mojtaba Amini Maryam Hosseinpour Kafshdouzsani Ali Akbari Sanjeev Gautam Cheol‐Hwee Shim Keun Hwa Chae 《应用有机金属化学》2018,32(9)
The magnetic CuFe2O4 nanoparticles have been synthesized and characterized by various spectroscopic methods, including X‐ray diffraction (XRD), O K, Cu and Fe K ‐edge X‐ray absorption near edge structure (XANES), energy dispersive X‐ray analysis (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The azide‐alkyne cycloaddition by the reaction of various phenylacetylenes with a mixture of benzyl halides and NaN3 and also three component (A3) coupling reaction of aldehyde, alkyne and amine catalyzed by CuFe2O4 nanoparticles under aerobic conditions led to the formation of the 1,4‐disubstituted‐1,2,3‐triazoles and propargylamines in excellent yields. The catalyst can be recovered by applying an external magnetic field for the subsequent cycloaddition reactions and reused without any tangible loss in catalytic efficiency. 相似文献
944.
Maryam Nourian Farnaz Zadehahmadi Reihaneh Kardanpour Shahram Tangestaninejad Majid Moghadam Valiollah Mirkhani Iraj Mohammadpoor‐Baltork 《应用有机金属化学》2018,32(1)
The catalytic activity of magnetically recoverable MIL‐101 was investigated in the oxidation of alkenes to carboxylic acids and cyanosilylation of aldehydes. MIL‐101 was treated with Fe3O4 and the prepared catalyst was characterized using Fourier transform infrared spectroscopy, X‐ray diffraction, N2 adsorption measurements, field emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy and inductively coupled plasma analysis. The catalytic active sites in this heterogeneous catalyst are Cr3+ nodes of the MIL‐101 framework. This heterogeneous catalyst has the advantages of excellent yields, short reaction times and reusability several times without significant decrease in its initial activity and stability in both oxidation and cyanosilylation reactions. Its magnetic property allows its easy separation using an external magnetic field. 相似文献
945.
A Cu(II) complex supported on Fe3O4@SiO2 core–shell magnetic nanoparticles (MNPs) was prepared and characterized by FT-IR, XRD, SEM, EDX, TEM, VSM, TGA, and AAS analysis. The load of Cu on picolinimidoamide ligand anchored on Fe3O4@SiO2 core–shell MNPs was determined as 1.22, 1.54, and 1.70 wt% using AAS, EDX and TGA analyses, respectively. Synthesized Cu(II) complex on Fe3O4@SiO2 MNPs efficiently catalyzed a click reaction between alkyl halides, alkynes, and sodium azide to synthesize corresponding triazoles in high to excellent yields. The catalyst was recovered using an external magnetic field, and recycled for subsequent reactions without substantial loss of efficiency. 相似文献
946.
Maryam Naseri Mohsen Mohammadniaei Koustuv Ghosh Subrata Sarkar Ravi Sankar Subhankar Mukherjee Souvik Pal Ehsan Ansari Dezfouli Arnab Halder Jixin Qiao Nabarun Bhattacharyya Yi Sun 《Electroanalysis》2023,35(2):e202200114
Heavy metals in drinking water have become a severe threat to human health. Detection of heavy metals has been achieved by electrochemical sensors that are modified with complex nanocomposites; however, reproducibility of these sensors is still a big challenge when applied in commercial settings. Here, a simple, very robust, and sensitive electrochemical sensor based on a screen-printed carbon electrode modified with butterfly-shaped silver nanostructure (AgNS/SPCE) has been developed for the concurrent determination of cadmium (II), lead (II), copper (II), and mercury (II) in water samples. The electrochemical behavior of the modified electrodes was investigated using cyclic voltammetry and differential pulse anodic stripping voltammetry. The AgNS/SPCE showed distinct peak potentials and a significant increase in the peak currents for all heavy metals, attributed to the high electrical conductivity and electrocatalytic activity of the synthesized butterfly-shaped AgNS. Moreover, the excellent stability and sensitivity towards simultaneous quantification of heavy metals have been obtained with detection limits of 0.4 ppb, 2.5 ppb, 7.3 ppb, and 0.7 ppb for Cd (II), Pb (II), Cu (II), and Hg (II), respectively. Besides, the constructed sensor was successfully applied to simultaneously quantify target heavy metals in spiked water samples. Owing to excellent sensitivity, high robustness, affordability, and fast response, the presented electrochemical sensor could be incorporated into a portable and miniaturized potentiostat device, making it a promising method for on-site water analysis. 相似文献
947.
Maryam Masoori Seyed Mohammad Mahdi Mortazavi Mohammad Vakili 《高分子科学杂志,A辑:纯化学与应用化学》2017,54(3):140-144
The effects of the type and concentration of comonomers 1-hexene and 1-octene in the copolymerization of ethylene were investigated using pre polymerized Ziegler-Natta (catalyst a) and without pre polymerized (catalyst b) catalysts in the presence of hydrogen as a chain transfer agent. The properties of produced polymers were characterized by a set of techniques: (SEM), (EDX), (DSC), (GPC). TIBA and DEAC were used as co catalysts. The results of microscopic and SEM images showed the morphology and structure of catalysts (a) and (b) and the obtained spherical polymers. In the presence of 1-hexene, activity of catalyst (a) was at its maximum. The comonomer 1-octene at 32 mmol presented its activity (1.7 × 103 g polymer/(g cat.h)) and after that, the activities decreased. Copolymerization of ethylene and 1-hexene by catalyst (b) showed higher activity (1.6 × 103 g polymer/ polymer/(g cat.h)) at 40 mmol concentration of 1-hexene in comparison to catalyst (a). 相似文献
948.
Mohamed Atia Dóra Bogdán Maryam Brügger Norbert Haider Péter Mátyus 《Tetrahedron》2017,73(23):3231-3239
Ethyl 4-oxo-3,4-dihydroquinazoline-2-carboxylate reacts selectively with trimethylaluminium-activated 2-amino- or 4-aminobenzoic acid ethyl esters to give the corresponding anilides without self-condensation of the aminobenzoate building blocks. After propargylation, the quinazolinones were treated with Hendrickson's reagent, but only the para-substituted ester was found to undergo the expected [4 + 2] cycloaddition reaction, affording a new Luotonin A derivative. A different regioselectivity was observed with the ortho-substituted ester which affords a benzoxazinone under identical conditions. When the ester group in the ortho-substituted intermediate is replaced with a nitrile function, the outcome of the reaction with Hendrickson's reagent depends on the absence or presence of a base (DBU), yielding either a triphenylphosphonium-substituted iminobenzoxazine or a 4-cyano-substituted Luotonin A derivative. 相似文献
949.
Nafiseh Moazzen Mohammadreza Khanmohammadi Amir Bagheri Garmarudi Maryam Kazemipour Mehdi Ansari Dogaheh 《Journal of the Iranian Chemical Society》2017,14(3):671-680
Fourier transform infrared spectroscopy coupled with chemometrics was employed to detect packaging polylactic acid-based biocomposite samples adulterated with polypropylene (PP) 30–45% and linear low-density polyethylene 2–10%. Principal component analysis, soft independent modeling of class analogy (SIMCA) and partial least square discriminate analysis (PLS-DA) chemometric techniques were utilized to classify samples in different classes. Totally, 362 samples were modeled in three different classes (two adulterated and one non-adulterated). The obtained results revealed that PLS-DA is the most suitable chemometric approach for prediction of probable adulteration in biocomposite samples with reliable specificity and selectivity. It could provide 99% correct class prediction rate between non-adulterated biocomposite samples and adulterated ones, while SIMCA methods provided 73.33% prediction accuracy in classification. 相似文献
950.
Maryam Bordbar Somaye Jafari Ali Yeganeh-Faal Bahar Khodadadi 《Journal of the Iranian Chemical Society》2017,14(4):897-906
Mn-doped ZnO single-crystal micronuts were synthesized via hydrothermal method in an hexamethylenetetramine aqueous solution. These micronuts are of wurtzite crystal structure. The effects of Mn doping amount and precursor concentration on the structural, optical properties and photocatalytic activity have been investigated. The synthesized Mn-doped ZnO was characterized by X-ray powder diffraction, field emission scanning electron microscopy (FESEM), UV–Vis absorption and photoluminescence spectroscopy. The structural analyses based on X-ray diffraction revealed the absence of Mn-related secondary phases. According to FESEM results, the length of ZnO micronuts was in the range of 5–8 μm. The band gap energy increased on increasing Mn doping concentration. The photocatalytic activity was studied by degradation of methyl orange aqueous solution, which showed that the Mn-doped ZnO micronuts prepared in precursor concentration of 0.1 M and 4% Mn doping had the highest photocatalytic activity. The effects of crystal defect and band gap energy on photocatalytic activity of Mn-doped ZnO samples were studied in different precursors and Mn doping amounts. 相似文献